EP1124625B1 - Membranes contenant du polyethercetone sulfone et un autre polymere, leur procede de production et leur utilisation - Google Patents

Membranes contenant du polyethercetone sulfone et un autre polymere, leur procede de production et leur utilisation Download PDF

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Publication number
EP1124625B1
EP1124625B1 EP99948789A EP99948789A EP1124625B1 EP 1124625 B1 EP1124625 B1 EP 1124625B1 EP 99948789 A EP99948789 A EP 99948789A EP 99948789 A EP99948789 A EP 99948789A EP 1124625 B1 EP1124625 B1 EP 1124625B1
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EP
European Patent Office
Prior art keywords
membrane
polymer
mpa
sulfonated
fuel cells
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Expired - Lifetime
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EP99948789A
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German (de)
English (en)
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EP1124625A1 (fr
Inventor
Thomas Soczka-Guth
Christoph Padberg
Georg Frank
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BASF Fuel Cell GmbH
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Pemeas GmbH
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Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
    • B01D71/06—Organic material
    • B01D71/58—Other polymers having nitrogen in the main chain, with or without oxygen or carbon only
    • B01D71/62—Polycondensates having nitrogen-containing heterocyclic rings in the main chain
    • B01D71/64—Polyimides; Polyamide-imides; Polyester-imides; Polyamide acids or similar polyimide precursors
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/10—Fuel cells with solid electrolytes
    • H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
    • H01M8/1018—Polymeric electrolyte materials
    • H01M8/102—Polymeric electrolyte materials characterised by the chemical structure of the main chain of the ion-conducting polymer
    • H01M8/1025—Polymeric electrolyte materials characterised by the chemical structure of the main chain of the ion-conducting polymer having only carbon and oxygen, e.g. polyethers, sulfonated polyetheretherketones [S-PEEK], sulfonated polysaccharides, sulfonated celluloses or sulfonated polyesters
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
    • B01D71/06—Organic material
    • B01D71/52—Polyethers
    • B01D71/522—Aromatic polyethers
    • B01D71/5222—Polyetherketone, polyetheretherketone, or polyaryletherketone
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
    • B01D71/06—Organic material
    • B01D71/66—Polymers having sulfur in the main chain, with or without nitrogen, oxygen or carbon only
    • B01D71/68—Polysulfones; Polyethersulfones
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/10—Fuel cells with solid electrolytes
    • H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
    • H01M8/1018—Polymeric electrolyte materials
    • H01M8/102—Polymeric electrolyte materials characterised by the chemical structure of the main chain of the ion-conducting polymer
    • H01M8/1027—Polymeric electrolyte materials characterised by the chemical structure of the main chain of the ion-conducting polymer having carbon, oxygen and other atoms, e.g. sulfonated polyethersulfones [S-PES]
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/10—Fuel cells with solid electrolytes
    • H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
    • H01M8/1018—Polymeric electrolyte materials
    • H01M8/102—Polymeric electrolyte materials characterised by the chemical structure of the main chain of the ion-conducting polymer
    • H01M8/1032—Polymeric electrolyte materials characterised by the chemical structure of the main chain of the ion-conducting polymer having sulfur, e.g. sulfonated-polyethersulfones [S-PES]
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/10—Fuel cells with solid electrolytes
    • H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
    • H01M8/1018—Polymeric electrolyte materials
    • H01M8/1039—Polymeric electrolyte materials halogenated, e.g. sulfonated polyvinylidene fluorides
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/10—Fuel cells with solid electrolytes
    • H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
    • H01M8/1018—Polymeric electrolyte materials
    • H01M8/1041—Polymer electrolyte composites, mixtures or blends
    • H01M8/1044—Mixtures of polymers, of which at least one is ionically conductive
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/10—Fuel cells with solid electrolytes
    • H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
    • H01M8/1018—Polymeric electrolyte materials
    • H01M8/1067—Polymeric electrolyte materials characterised by their physical properties, e.g. porosity, ionic conductivity or thickness
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/10—Fuel cells with solid electrolytes
    • H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
    • H01M8/1018—Polymeric electrolyte materials
    • H01M8/1069—Polymeric electrolyte materials characterised by the manufacturing processes
    • H01M8/1081—Polymeric electrolyte materials characterised by the manufacturing processes starting from solutions, dispersions or slurries exclusively of polymers
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30—Hydrogen technology
    • Y02E60/50—Fuel cells
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50—Manufacturing or production processes characterised by the final manufactured product

Definitions

  • Fuel cells are electrochemical energy converters, which are characterized by their high efficiency.
  • Polymer electrolyte fuel cells (PEMs) are distinguished by their high power density and low power-to-weight ratio among the various types of fuel cells.
  • Polyether ketones consisting predominantly of the repeating unit -O-Ar-CO-Ar are disclosed in EP-A-0 152 161; sulfonated, strictly alternating polyether ketones with the repeating unit -O-Ar-CO-Ar- in J. Polym. Sci .: Vol. 23, 2205-2223, 1985.
  • the structure of the polyether ketones is done here by electrophilic, and not as described in EP 0152161 by nucleophilic attack.
  • the polymers are sulfonated using sulfur trioxide using triethyl phosphate in dichloroethane.
  • Another sulfonation method used in the literature is chlorosulfonation with chlorosulfonic acid.
  • degradation of the molecular weight is also observed in this method. It concludes the amidation of Acid chlorides.
  • the use in fuel cells or property profiles, which might suggest the use in fuel cells are not mentioned.
  • a little-studied polyether ketone is the mentioned, strictly aging polymer having the empirical formula -O-Ar-CO-Ar-, which is produced, inter alia, by Victrex Plc, Great Britain.
  • the sulfonation of the polymer may, for. B. be achieved by the addition of oleum to the sulfuric acid solution of the polymer.
  • the suitability of such aromatic, non-fluorinated polymers for use in fuel cells is in the known literature, however, due to insufficient stability of the polymer membranes under the extreme conditions prevailing in fuel cells, contested (A. Steck, Proc. 1 st Inter. Symp. On New Materials For Fuel Cell Systems, Montreal 1995, pp 74).
  • the glass transition temperature of PEK (141 ° C., see EP 0 152 161 B1) differs only insignificantly compared to PEEK (143 ° C.), crystallinity 30%.
  • sulfonated polyether ketones are based on of Victrex PEK with a comparable IEC, stable in boiling water for more than 50 h.
  • the electron-deficient structure of the polyether ketone polymer backbone due to the absence of -O-Ar-O units appears to be particularly suitable for fuel cell applications.
  • Highly sulfonated polymer membranes are of particular interest for low or no humidification fuel cells, but also for so-called super-cap capacitors.
  • EP-A-0688 824 mentions membranes of homogeneous polymer alloys based on polyether ketones, polyether sulfones and a third, hydrophilic polymer. The addition of the third hydrophilic polymer is necessary to achieve sufficient humidifying properties of the polymers.
  • the object of the present invention is to provide high-performance membranes with high proton conductivity from cost-effective materials, which furthermore have high chemical and mechanical stability and are therefore particularly suitable for use in fuel cells.
  • the performance of the material in the fuel cell should be superior to previous standard fluorinated materials such as Nafion.
  • the present invention solves this problem and relates to membranes containing 30-99, preferably 55 to 99 wt.%, Of a sulfonated, strictly alternating polyether ketone (A) having repeating units of the formula (I) -Ar-O-Ar'-CO-, wherein Ar and Ar 'are independently divalent aromatic radicals, Ar is preferably a phenylene radical having para and / or meta bonds and Ar 'is preferably a phenylene, naphthylene, biphenylene, anthrylene radical having an ion exchange capacity of 1.3 to 4.0 meq (-SO 3 H) / g (polymer) and 0.5-70% by weight, in particular 1.0 to 50% by weight, of a partially, non or perfluorinated polyethersulfone, polyimide or a derivative of these polymers (B), which is preferably soluble in organic solvents.
  • A sulfonated, strictly alternating polyether ketone having repeating units of the formula (
  • the ion exchange capacity (hereinafter "IEC") is determined by elemental analysis of the washed and dried polymers by determining the ratio of carbon to sulfur (C / S quotient).
  • Soluble polymers in the sense of this description are polymers which are soluble at 25 ° C. to at least 0.1 g per liter in organic solvents.
  • the second polymer (B) such as a polyethersulfone of the formula -Ar-O-Ar'-SO 2 - or a polyimide or a derivative of these polymers, can be mixed with the sulfonated polyether ketones, without that the conductivity breaks down.
  • the second polymer (B) such as a polyethersulfone of the formula -Ar-O-Ar'-SO 2 - or a polyimide or a derivative of these polymers
  • the polymers used according to the invention preferably contain aromatic radicals which optionally bear substituents, such as alkyl, cycloalkyl, aryl or halogen.
  • the E modulus in water at 60 ° C is significantly improved (see examples), which has a positive effect on the strength under the influence of differential pressure and at the edges of the membrane, where the humidified gases unhindered and without mechanical support by the Electrode to the membrane can affect.
  • the modulus of elasticity at 60 ° C in water increases up to 540 MPa compared to 7 MPa for the pure material with still very good conductivity values.
  • the performance in the fuel cell is good for these membrane materials, as shown in the examples.
  • the modulus values are in comparison with the conventional polyether ketones, such as. Victrex® and Hostatec®, lower, but this results in a significantly improved elongation at break, which is crucial for a good stability and the use of the membranes in fuel cells.
  • the membranes of the invention are characterized in that they have an elongation at break of ⁇ 200 in an E modulus (determined as the slope of the tangent at 1.2 MPa) in water at 60 ° C of at least 90 MPa, in particular 100 to 700 MPa %, in particular 200 to 800%.
  • the membranes of the invention are therefore ideal for use in fuel cells, in particular for direct methanol fuel cells, or high performance capacitors and for use in electrodialysis, the membrane in the latter case preferably has a thickness of at least 30 microns.
  • a content of 5 to 25 wt.% Of the polymer (B) for use in direct methanol fuel cells, a content of 5 to 50 wt.% Preferably.
  • the sulfonated polyether ketone (A) is reacted with the polymer (B) in a weight ratio in the range of 0.01 to 0.5 (B / A) in a solvent such as N-methylpyrrolidone (NMP) or dimethylformamide (DMF), dimethylacetamide (DMAc), dimethyl sulfoxide (DMSO) or solvent mixtures containing water and 1,4-dioxane and acetonitrile, in Solution brought.
  • NMP N-methylpyrrolidone
  • DMF dimethylformamide
  • DMAc dimethylacetamide
  • DMSO dimethyl sulfoxide
  • solvent mixtures containing water and 1,4-dioxane and acetonitrile in Solution brought.
  • the temperature should preferably not exceed 90 ° C.
  • the solution is filtered at a temperature in the range of 20 to ⁇ 90 ° C over a PP (polypropylene) depth filter and then dried and degassed.
  • the solution is spread by means of a stainless steel blade on a flat support, such as a glass plate and dried at 25 to 140 ° C in a circulating air heat chamber overnight.
  • a stainless steel blade on a flat support, such as a glass plate and dried at 25 to 140 ° C in a circulating air heat chamber overnight.
  • the membrane is dried so that the residual content of solvent is less than 0.5 wt.%.
  • the membrane be free of residual solvent and other water-soluble impurities after washing by washing in water or a dilute acid (nitric acid, sulfuric acid, phosphoric acid) at a concentration of 0.1-20%.
  • a dilute acid nitric acid, sulfuric acid, phosphoric acid
  • the solution of the blend can be introduced into an absorbent fleece.
  • the conductivity of the composite thus produced for protons in this case is in contact with water at room temperature greater than 50 mS / cm.
  • the polymer is filtered off, washed neutral (test with BaCl 2 solution) and dried at 60-120 ° C in a convection oven.
  • Example 2 Production of the Blends Using the Example of the Membrane Used in Example 3
  • the solutions are prepared in a heatable Doppelmanteigefäß under nitrogen overflow.
  • a heatable Doppelmanlessnessefäß under nitrogen overflow.
  • 332 g of dry NMP 8.5 g of dry polyethersulfone Ultrason® 7020 P and 52.7 g of dry, sulfonated polyether ketone PEK with an IEC of 2.12 meq (-SO 3 H) / g (polymer) introduced and brought into solution with a dissolver.
  • the temperature of the solution should not exceed 90 ° C.
  • the solution is filtered at 80 ° C over a PP depth filter (5 microns) and for 10 min. Degassed in a vacuum oven at 50 ° C, 100 mbar.
  • the solution is spread on a glass plate with the aid of a stainless steel squeegee (200 ⁇ m) and dried overnight at 30 to 120 ° C in a circulating air heat chamber.
  • Proton conductivity values of PEK / PES blends (PEK with an IEC of 2.12 meq (-SO 3 H) / g (polymer).) The proton conductivity is measured with a 4-pole arrangement.
  • the electrode material used is platinum
  • the temperature and width of the membrane are determined in the dry state after treatment with 5% nitric acid at 40 ° C.
  • the measuring instrument used is a toothed IM 5d, converted for measurement in a 4-pole arrangement.
  • Example 7 Comparative Data, Mechanics

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Electrochemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Sustainable Development (AREA)
  • Sustainable Energy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Composite Materials (AREA)
  • Dispersion Chemistry (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Fuel Cell (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)
  • Polyethers (AREA)
  • Moulding By Coating Moulds (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)

Claims (10)

  1. Des membranes consistant en 30 - 99,5 % en poids d'une polyéthercétone sulfonée, rigoureusement alternée (A) avec des unités de répétition de la formule (I) -Ar-O-Ar'-CO-, où Ar et Ar' sont deux restes aromatiques, bivalents, indépendantes l'un de l'autre, avec une capacité d'échangeur d'ions de 1,3 jusqu'à 4,0 milliéquivalents (-SO3H)/g (polymère) et 0,5 - 70 % en poids d'une polyéthersulfone totalement, partiellement ou pas du tout perfluorurée, une polyimide ou un dérivé de ces polymères.
  2. Membrane selon la revendication 1, où Ar est un reste de phénylène avec des liaisons para- et/où meta- et Ar' est un reste de phénylène-, naphtylène-, diphénilène- ou anthrylène.
  3. Membrane selon la revendication 1, où le polymère totalement, partiellement ou pas du tout perfluoruré (B) est un polymère soluble dans des solvants organiques.
  4. Membrane selon la revendication 1, où le polymèrere (B) est une polyéthersulfone de la formule -Ar-O-Ar'-SO2- où Ar et Ar' ont la signification définie dans la revendication 1.
  5. Membrane selon l'une quelconque des revendications 1 jusqu'à 4, où le module d'élasticité à l'état seché à 23° C, 50 % humidité relative est ≥ 600 MPa.
  6. Membrane selon l'une quelconque des revendications 1 jusqu'à 5, où le module d'élasticité (déterminé comme accroissement de la tangente à 1,2 MPa) a une valeur dans l'eau à 60° C de minimum 90 MPa, et l'élongation de rupture est ≥ 200 %.
  7. Procédé pour produire une membrane selon les revendications 1 jusqu'à 5, par la dissolution dans un solvant d'une polyéthercétone sulfonée (A) avec des unités de répétition de la formule (I) comme définit dans la revendication 1, avec une polyéthersulfone totalement, partiellement ou pas du tout perfluorurée, une polyimide, ou un dérivé de ces polymères (B) dans une proportion pondérale qui se trouve dans l'intervalle à partir de 0,01 jusqu'à 0,5 (B/A), la filtration, l'application de la solution sur une surface portante plane à fin de se sécher ensuite à une température de 25 jusqu'à 140° C.
  8. L'utilisation de la membrane selon les revendications 1 jusqu'à 6 pour son application dans des piles à combustion, particulièrement dans des piles à combustion directe du méthanol.
  9. L'utilisation de la membrane selon les revendications 1 jusqu'à 6 dans des condensateurs de grande performance.
  10. L'utilisation de la membrane selon les revendications 1 jusqu'à 6 avec une épaisseur de minimum 30 µm pour son application dans l'électrodialyse.
EP99948789A 1998-10-16 1999-09-18 Membranes contenant du polyethercetone sulfone et un autre polymere, leur procede de production et leur utilisation Expired - Lifetime EP1124625B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE19847782A DE19847782A1 (de) 1998-10-16 1998-10-16 Verfahren zum Betrieb einer Brennstoffzelle
DE19847782 1998-10-16
PCT/EP1999/006929 WO2000023177A1 (fr) 1998-10-16 1999-09-18 Membranes contenant du polyethercetone sulfone et un autre polymere, leur procede de production et leur utilisation

Publications (2)

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EP1124625A1 EP1124625A1 (fr) 2001-08-22
EP1124625B1 true EP1124625B1 (fr) 2006-06-21

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EP99948789A Expired - Lifetime EP1124625B1 (fr) 1998-10-16 1999-09-18 Membranes contenant du polyethercetone sulfone et un autre polymere, leur procede de production et leur utilisation

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Country Link
US (1) US6914084B1 (fr)
EP (1) EP1124625B1 (fr)
JP (1) JP4540850B2 (fr)
KR (1) KR100646152B1 (fr)
CN (1) CN1165368C (fr)
AT (1) ATE330696T1 (fr)
BR (1) BR9914597A (fr)
CA (1) CA2347090C (fr)
DE (2) DE19847782A1 (fr)
MY (1) MY130729A (fr)
WO (1) WO2000023177A1 (fr)

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Publication number Priority date Publication date Assignee Title
DE10047551B4 (de) * 2000-09-22 2004-04-08 Gkss-Forschungszentrum Geesthacht Gmbh Direct Methanol Fuel Cell-Membran
DE10052242A1 (de) * 2000-10-21 2002-05-02 Celanese Ventures Gmbh Mit Säure dotierte, ein- oder mehrschichtige Kunststoffmembran mit Schichten aufweisend Polymerblends umfassend Polymere mit wiederkehrenden Azoleinheiten, Verfahren zur Herstellung solche Kunststoffmembranen sowie deren Verwendung
AU2002241152B2 (en) 2001-03-21 2008-02-28 Victrex Manufacturing Limited Polymer electrolyte membrane fuel cell
KR100746339B1 (ko) * 2006-03-07 2007-08-03 한국과학기술원 고분자 전해질 연료전지용 복합막의 제조방법
ITMI20071034A1 (it) * 2007-05-23 2008-11-24 St Microelectronics Srl Sintesi e caratterizzazione di una nuova membrana a scambio protonico (pem) per applicazioni in celle a combustibile
US8341167B1 (en) 2009-01-30 2012-12-25 Intuit Inc. Context based interactive search
KR20120114271A (ko) * 2009-12-04 2012-10-16 프루덴트 에너지 인코포레이티드 폴리머 혼합 양성자 교환막 및 이의 제조방법
WO2015090571A1 (fr) 2013-12-19 2015-06-25 Treofan Germany Gmbh & Co. Kg MEMBRANE ÉCHANGEUSE D'IONS COMPOSÉE D'UN FILM POREUX β ÉTIRÉ BIAXIALEMENT
FR3016477B1 (fr) * 2014-01-16 2017-09-08 Commissariat Energie Atomique Membrane pour pile a combustible a membrane echangeuse de protons
RS59961B1 (sr) 2014-06-16 2020-03-31 Core Energy Recovery Solutions Inc Mešovite membrane za transport vodene pare i postupci za izradu istih

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US4816556A (en) * 1985-02-22 1989-03-28 E. I. Du Pont De Nemours And Company Ordered polyetherketones
GB2216134B (en) 1988-03-29 1992-08-12 Paterson Candy Int Membranes and methods of preparation thereof
US5049340A (en) * 1989-12-18 1991-09-17 E. I. Du Pont De Nemours And Company Process for making continuous films of ordered poly(ether ketone ketones)
KR930006259B1 (ko) * 1990-02-02 1993-07-09 한국과학기술원 새로운 방향족 폴리술폰에테르케톤 중합체
SG73410A1 (en) 1992-06-13 2000-06-20 Hoechst Ag Polymer electrolyte membrane and process for the production thereof
EP0604882B1 (fr) 1992-12-30 1998-08-26 Hoechst Aktiengesellschaft Membranes semi-perméables d'alliages polymères miscibles homogènes
DE4415678A1 (de) 1994-05-04 1995-11-09 Hoechst Ag Elektrochemische Zelle
DE4422158A1 (de) * 1994-06-24 1996-01-04 Hoechst Ag Homogene Polymerlegierungen auf der Basis von sulfonierten, aromatischen Polyetherketonen
WO1996029360A1 (fr) 1995-03-20 1996-09-26 Hoechst Aktiengesellschaft Cetones polyether sulfonees, leur procede de production et leur utilisation pour fabriquer des membranes

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Publication number Publication date
MY130729A (en) 2007-07-31
CA2347090A1 (fr) 2000-04-27
KR20010075627A (ko) 2001-08-09
JP2002527233A (ja) 2002-08-27
CN1328484A (zh) 2001-12-26
EP1124625A1 (fr) 2001-08-22
CN1165368C (zh) 2004-09-08
BR9914597A (pt) 2001-06-26
ATE330696T1 (de) 2006-07-15
US6914084B1 (en) 2005-07-05
WO2000023177A1 (fr) 2000-04-27
JP4540850B2 (ja) 2010-09-08
DE59913610D1 (de) 2006-08-03
KR100646152B1 (ko) 2006-11-14
CA2347090C (fr) 2007-09-11
DE19847782A1 (de) 2000-04-20

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